Canonical Allele Identifier: CA400370571

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351032T>C (hg19) ; chr17:g.58273671T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273671T>C , CM000679.2:g.58273671T>C	GRCh38
NC_000017.10:g.56351032T>C , CM000679.1:g.56351032T>C	GRCh37
NC_000017.9:g.53706031T>C	NCBI36
NG_009629.1:g.12265A>G , LRG_84:g.12265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-2A>G
ENST00000699291.1:c.491-2A>G	ENSP00000514272.1:n.491-2A>G
ENST00000699292.1:n.404A>G
ENST00000225275.4:c.1366-2A>G MANE Select	ENSP00000225275.3:n.1366-2A>G
ENST00000225275.3:c.1366-2A>G	ENSP00000225275.3:n.1366-2A>G
NM_000250.1:c.1366-2A>G , LRG_84t1:c.1366-2A>G	NP_000241.1:n.1366-2A>G
XM_011524821.1:c.1552-2A>G	XP_011523123.1:n.1552-2A>G
XM_011524822.1:c.1081-2A>G	XP_011523124.1:n.1081-2A>G
XM_011524823.1:c.1391-2A>G	XP_011523125.1:n.1391-2A>G
NM_000250.2:c.1366-2A>G MANE Select	NP_000241.1:n.1366-2A>G